Tag | Content |
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EnhancerAtlas ID | HS133-12861 |
Organism | Homo sapiens |
Tissue/cell | melanoma |
Coordinate | chr17:48863970-48865160 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
TP53 | MA0106.3 | chr17:48864598-48864616 | GGCCTGCCCGGGCATGTT | - | 6.56 | TP53 | MA0106.3 | chr17:48864598-48864616 | GGCCTGCCCGGGCATGTT | + | 7.02 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_63310 | chr17:48862158-48886996 | NCI-H82 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH17I050785 | chr17 | 48862948 | 48864955 |
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Enhancer Sequence | CAAGTACCGA GACCTCTGAG GCAGGAGAGA GGGGAATGTG TTCGGGGGAT GAAAACAAGG 60 GCCAATGCAG CGGGAGCAGA GGGAGCTGGG GATTTCTGGG TGGGGCCATC AGGCAGGGCC 120 AGGCTGAGCC TTGGTGTTCT TCAGCTCAGA ACCCCTCACC TCCTCTCACT GACCCCCACC 180 CCATCCTCTG AGATCCGACC TCACAGCATA GTCAGATCCA ACCTCTTCTC CCCACCTCCG 240 CTGCGGCCAC CCTAGTCTGA TTATTGCAAT ATCCCCTCCC ATTCCCACTG GTCTCCCTGC 300 TTCTGCACCG CCCCCATATC TCTTCTTTCT CAGCAATAAA GTGATCCTTT TAGCATGGAA 360 GTCAGAGCTT GCCAGGCCTC TGCTTCTCAT TTTGCTTAGA GTAAGTGCCT AAGTCTTGCA 420 ATGGTCTACA AAGCCCTCCA CAGTCTGGAT CCCAGGAGCT CCTGCAACGT GGTCCCCTCT 480 CTCACTTGGC TGTAGCCCCA CTGGCCCTGT GCTCCTTCTC AAGTACACCA GGCAAGCCCC 540 TATCTGGAAG GAGGGCCTTT GCACTGCCCG TTCCCTTGGC CCGGAATGTT CTTTCCTCAC 600 ATATCCATGG GTCTCTCATC CTTCAGCAGG CCTGCCCGGG CATGTTCTCA TAGTGGAGCT 660 CAGGGCAAGA ACAGATGGAG ATGCTAAGCC CTCTTCTGCC TGCCTCCGGT CTGCTAACAT 720 CCTGCTGGCC ACAGCAAGCA CGTGGCTGAG CCCAGAGTCT GAGTGGGAGG GCACCAGGAT 780 GGTAGATGCA CACGGTAAAG ACACAGGGAG TAAAGCACTG GGGCCCTTGC ACACATGATT 840 ACAGCCCCTT GATCTGAGCT CCAAATCCCA GGCCTCCTCC TGCACAGCGA CCTGCCACCA 900 TCAGTAACTC TCTCCACCAG CCACCATCCC ATTTTCATTC AGCAAACATT TGTGGAGCAC 960 CTGCAGTGTG CAGGCCCTGT TCTAGACACT GTGAGGCAGC TGCACATAAA GTAGACGAAG 1020 GCCCTGCCCT TTTAAAGTTT TGTTTTGTTT TTTTTTCTTT TTTTTTTTTT TCGAGACAGA 1080 GTCTCTCTCT GTCGTCCAGG CTGGAGTGCA GTGGTGCGAC CTCGGCTCAC TGCAATCTCT 1140 GCCTGTTGGG TTCAAGTGAT TCTCCCATCT ACTCGGGAGG CTGAGGTAGG 1190
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